MA53352A - Dérivés de pyridin-2-(1h)-one-quinolinone en tant qu'inhibiteurs d'isocitrate déshydrogénase - Google Patents
Dérivés de pyridin-2-(1h)-one-quinolinone en tant qu'inhibiteurs d'isocitrate déshydrogénaseInfo
- Publication number
- MA53352A MA53352A MA053352A MA53352A MA53352A MA 53352 A MA53352 A MA 53352A MA 053352 A MA053352 A MA 053352A MA 53352 A MA53352 A MA 53352A MA 53352 A MA53352 A MA 53352A
- Authority
- MA
- Morocco
- Prior art keywords
- pyridin
- isocitrate dehydrogenase
- dehydrogenase inhibitors
- quinolinone derivatives
- quinolinone
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/47—Quinolines; Isoquinolines
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/47—Quinolines; Isoquinolines
- A61K31/472—Non-condensed isoquinolines, e.g. papaverine
- A61K31/4725—Non-condensed isoquinolines, e.g. papaverine containing further heterocyclic rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US201462053006P | 2014-09-19 | 2014-09-19 | |
US201562128089P | 2015-03-04 | 2015-03-04 | |
US201562150812P | 2015-04-21 | 2015-04-21 |
Publications (1)
Publication Number | Publication Date |
---|---|
MA53352A true MA53352A (fr) | 2021-09-15 |
Family
ID=54291606
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
MA040481A MA40481A (fr) | 2014-09-19 | 2015-09-18 | Dérivés de pyridin-2-(1h)-one-quinolinone à titre d'inhibiteurs d'isocitrate déshydrogénase mutante |
MA053352A MA53352A (fr) | 2014-09-19 | 2015-09-18 | Dérivés de pyridin-2-(1h)-one-quinolinone en tant qu'inhibiteurs d'isocitrate déshydrogénase |
Family Applications Before (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
MA040481A MA40481A (fr) | 2014-09-19 | 2015-09-18 | Dérivés de pyridin-2-(1h)-one-quinolinone à titre d'inhibiteurs d'isocitrate déshydrogénase mutante |
Country Status (36)
Country | Link |
---|---|
US (8) | US9834539B2 (fr) |
EP (4) | EP4257131A3 (fr) |
JP (1) | JP6648115B2 (fr) |
KR (1) | KR102209667B1 (fr) |
CN (3) | CN117695280A (fr) |
AU (3) | AU2015317329B2 (fr) |
BR (1) | BR112017005238B1 (fr) |
CA (1) | CA2961817C (fr) |
CL (1) | CL2017000658A1 (fr) |
CO (1) | CO2017003241A2 (fr) |
CY (2) | CY1121149T1 (fr) |
DK (2) | DK3447050T3 (fr) |
EA (1) | EA034336B1 (fr) |
EC (1) | ECSP17022933A (fr) |
ES (3) | ES2953347T3 (fr) |
FI (1) | FI3733662T3 (fr) |
HR (1) | HRP20200666T1 (fr) |
HU (2) | HUE062424T2 (fr) |
IL (3) | IL292608A (fr) |
LT (2) | LT3194376T (fr) |
MA (2) | MA40481A (fr) |
ME (1) | ME03776B (fr) |
MX (2) | MX2017003404A (fr) |
MY (2) | MY176250A (fr) |
NZ (2) | NZ730373A (fr) |
PE (1) | PE20171056A1 (fr) |
PH (1) | PH12017500517A1 (fr) |
PL (3) | PL3194376T3 (fr) |
PT (3) | PT3194376T (fr) |
RS (2) | RS60140B1 (fr) |
SA (1) | SA517381129B1 (fr) |
SG (1) | SG11201702194SA (fr) |
SI (2) | SI3194376T1 (fr) |
TW (1) | TWI686390B (fr) |
WO (1) | WO2016044789A1 (fr) |
ZA (2) | ZA201702127B (fr) |
Families Citing this family (24)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102985557B (zh) | 2009-03-13 | 2018-06-15 | 安吉奥斯医药品有限公司 | 用于细胞增殖相关病症的方法和组合物 |
EP2491145B1 (fr) * | 2009-10-21 | 2016-03-09 | Agios Pharmaceuticals, Inc. | Procédés et compositions pour des troubles relatifs à la prolifération cellulaire |
EP3406609A1 (fr) | 2014-02-06 | 2018-11-28 | Heptares Therapeutics Limited | Composés aza bicycliques en tant qu'agonistes du récepteur muscarinique |
AU2015317321B2 (en) * | 2014-09-19 | 2020-03-12 | Forma Therapeutics, Inc. | Quinolinone pyrimidines compositions as mutant-isocitrate dehydrogenase inhibitors |
CA2961807A1 (fr) | 2014-09-19 | 2016-03-24 | Forma Therapeutics, Inc. | Derives de phenylquinoleinone en tant qu'inhibiteurs d'isocitrate deshydrogenase mutante |
ES2953347T3 (es) | 2014-09-19 | 2023-11-10 | Forma Therapeutics Inc | Derivados de piridin-2(1H)-ona quinolinona como inhibidores de isocitrato deshidrogenasa mutante |
MA39484A (fr) | 2014-09-19 | 2016-03-24 | Bayer Pharma AG | Indazoles à substituants benzyle utilisés comme inhibiteurs de bub1 |
MX2017003626A (es) | 2014-09-19 | 2018-01-24 | Forma Therapeutics Inc | Derivados de piridinil quinolinona como inhibidores de isocitrato deshidrogenasa mutante (mt-idh). |
ES2905564T3 (es) * | 2014-12-22 | 2022-04-11 | Us Health | Inhibidores mutantes de IDH1 útiles para tratar el cáncer |
WO2016171755A1 (fr) | 2015-04-21 | 2016-10-27 | Forma Therapeutics, Inc. | Dérivés de phénylquinoléinone en tant qu'inhibiteurs de l'isocitrate déshydrogénase mutante |
WO2016171756A1 (fr) | 2015-04-21 | 2016-10-27 | Forma Therapeutics, Inc. | Composés hétérocycliques de quinoléinone à cinq chaînons comme inhibiteurs de l'isocitrate déshydrogénase mutante |
PL3619196T3 (pl) | 2017-05-04 | 2022-08-29 | Bayer Cropscience Aktiengesellschaft | Pochodne 2-{[2-(fenyloksymetylo)pirydyn-5-yl]oksy}-etanoaminy i związki pokrewne jako środki do zwalczania szkodników np. do ochrony upraw |
US20210196701A1 (en) | 2018-05-16 | 2021-07-01 | Forma Therapeutics, Inc. | Inhibiting mutant idh-1 |
PL3720442T3 (pl) | 2018-05-16 | 2023-05-29 | Forma Therapeutics, Inc. | Hamowanie mutanta idh-1 |
US11013734B2 (en) | 2018-05-16 | 2021-05-25 | Forma Therapeutics, Inc. | Treating patients harboring an isocitrate dehydrogenase-1 (IDH-1) mutation |
US10532047B2 (en) | 2018-05-16 | 2020-01-14 | Forma Therapeutics, Inc. | Solid forms of ((S)-5-((1-(6-chloro-2-oxo-1,2-dihydroquinolin-3-yl)ethyl)amino)-1-methyl-6-oxo-1,6-dihydropyridine-2-carbonitrile |
US11311527B2 (en) | 2018-05-16 | 2022-04-26 | Forma Therapeutics, Inc. | Inhibiting mutant isocitrate dehydrogenase 1 (mIDH-1) |
WO2020232381A1 (fr) | 2019-05-16 | 2020-11-19 | Forma Therapeutics, Inc. | Inhibition de l'isocitrate déshydrogénase 1 mutante (midh-1) |
US11013733B2 (en) | 2018-05-16 | 2021-05-25 | Forma Therapeutics, Inc. | Inhibiting mutant isocitrate dehydrogenase 1 (mlDH-1) |
TW202104207A (zh) * | 2019-04-17 | 2021-02-01 | 美商健生生物科技公司 | 二氫乳清酸脫氫酶抑制劑 |
US11566013B1 (en) * | 2019-11-20 | 2023-01-31 | Forma Therapeutics, Inc. | Inhibiting mutant isocitrate dehydrogenase 1 (mIDH1) |
CN112321571B (zh) * | 2020-10-27 | 2022-06-03 | 浙江工业大学 | 2-呋喃-喹啉-4-甲酰胺类化合物及其应用 |
CN112341389B (zh) * | 2020-10-27 | 2022-07-29 | 浙江工业大学 | 一种含氮芳杂环取代的喹啉甲酰胺类衍生物及其应用 |
CN115850240B (zh) * | 2022-12-28 | 2023-09-19 | 北京康立生医药技术开发有限公司 | 一种治疗急性髓系白血病药物奥卢他西尼的合成方法 |
Family Cites Families (40)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
IL99731A0 (en) | 1990-10-18 | 1992-08-18 | Merck & Co Inc | Hydroxylated pyridine derivatives,their preparation and pharmaceutical compositions containing them |
US5262564A (en) | 1992-10-30 | 1993-11-16 | Octamer, Inc. | Sulfinic acid adducts of organo nitroso compounds useful as retroviral inactivating agents anti-retroviral agents and anti-tumor agents |
US20030105124A1 (en) | 2000-04-27 | 2003-06-05 | Susan Beth Sobolov-Jaynes | Substituted benzolactam compounds |
EP1534703A2 (fr) | 2002-06-12 | 2005-06-01 | Abbott Laboratories | Antagonistes du recepteur de l'hormone de melano-concentration |
WO2004043936A1 (fr) | 2002-11-14 | 2004-05-27 | Kyowa Hakko Kogyo Co., Ltd. | Inhibiteurs de plk (kinases du type polo) |
RU2284325C2 (ru) | 2003-12-17 | 2006-09-27 | Общество С Ограниченной Ответственностью "Асинэкс Медхим" | Производные фенил-3-аминометил-хинолона-2 в качестве ингибиторов no-синтетазы, способ их получения, биологически активные соединения и фармацевтическая композиция на их основе |
US7956060B2 (en) | 2004-03-30 | 2011-06-07 | Kyowa Hakko Kirin Co., Ltd. | Pyrimidine derivative compound |
WO2006054912A1 (fr) * | 2004-11-18 | 2006-05-26 | Obchestvo S Ogranichennoy Otvetstvennost'u 'asineks Medhim' | Derives d'aryl(hetaryl)-3-aminomethylchinolone-2 utilises en tant qu'inhibiteurs de no-synthetase et de cyclo-oxygenase-2, procedes de leur fabrication et compositions pharmaceutiques sur leur base |
TW200803855A (en) | 2006-02-24 | 2008-01-16 | Kalypsys Inc | Quinolones useful as inducible nitric oxide synthase inhibitors |
CA2657287A1 (fr) * | 2006-07-17 | 2008-01-24 | Merck & Co., Inc. | Composes de 1-hydroxy naphtyridine en tant qu'agents anti-vih |
JP2010043004A (ja) | 2006-12-06 | 2010-02-25 | Dainippon Sumitomo Pharma Co Ltd | 新規2環性複素環化合物 |
JP5450381B2 (ja) | 2007-04-30 | 2014-03-26 | プロメティック・バイオサイエンスィズ・インコーポレーテッド | 化合物、そのような化合物を含有する組成物、及びそのような化合物を用いるがん及び自己免疫疾患の治療法 |
JP2012529511A (ja) | 2009-06-08 | 2012-11-22 | アブラクシス バイオサイエンス リミテッド ライアビリティー カンパニー | トリアジン誘導体類及びそれらの治療応用 |
WO2011072174A1 (fr) * | 2009-12-09 | 2011-06-16 | Agios Pharmaceuticals, Inc. | Composés thérapeutiquement actifs destinés au traitement d'un cancer caractérisé par une mutation idh |
WO2012006104A2 (fr) | 2010-06-28 | 2012-01-12 | Academia Sinica, Taiwan | Composés et procédés destinés au traitement d'une infection par la tuberculose |
CN102558049B (zh) * | 2010-12-17 | 2015-02-04 | 中国科学院上海药物研究所 | 一类双香豆素类化合物及其制备方法和用途 |
US20120184562A1 (en) | 2011-01-19 | 2012-07-19 | Kin-Chun Luk | 1,6- and 1,8-naphthyridines |
US20120184548A1 (en) | 2011-01-19 | 2012-07-19 | Romyr Dominique | Carboxylic acid aryl amides |
WO2012129562A2 (fr) | 2011-03-24 | 2012-09-27 | The Scripps Research Institute | Composés et procédés pour l'induction de la chondrogenèse |
CN102827170A (zh) | 2011-06-17 | 2012-12-19 | 安吉奥斯医药品有限公司 | 治疗活性组合物和它们的使用方法 |
CN103814020B (zh) * | 2011-06-17 | 2017-07-14 | 安吉奥斯医药品有限公司 | 治疗活性组合物和它们的使用方法 |
CA2849995A1 (fr) | 2011-09-27 | 2013-04-04 | Novartis Ag | 3-pyrimidin-4-yl-oxazolidin-2-ones comme inhibiteurs d'idh mutante |
CN104271132B (zh) | 2011-12-21 | 2018-01-12 | 科罗拉多大学董事会法人团体 | 靶向Ral GTP酶的抗癌化合物及使用其的方法 |
MX358940B (es) | 2012-01-06 | 2018-09-10 | Agios Pharmaceuticals Inc Star | Compuestos terapéuticamente activos y sus métodos de uso. |
BR112015022483A2 (pt) * | 2013-03-14 | 2017-07-18 | Novartis Ag | 3-pirimidin-4-il-oxazolidin-2-onas como inibidores de idh mutante |
US10478445B2 (en) | 2013-07-03 | 2019-11-19 | Georgetown University | Boronic acid derivatives of resveratrol for activating deacetylase enzymes |
CA2939026A1 (fr) | 2014-02-11 | 2015-08-20 | Bayer Pharma Aktiengesellschaft | Benzimidazol-2-amines en tant qu'inhibiteurs midh1 |
AU2015317321B2 (en) | 2014-09-19 | 2020-03-12 | Forma Therapeutics, Inc. | Quinolinone pyrimidines compositions as mutant-isocitrate dehydrogenase inhibitors |
CA2961807A1 (fr) | 2014-09-19 | 2016-03-24 | Forma Therapeutics, Inc. | Derives de phenylquinoleinone en tant qu'inhibiteurs d'isocitrate deshydrogenase mutante |
MX2017003626A (es) | 2014-09-19 | 2018-01-24 | Forma Therapeutics Inc | Derivados de piridinil quinolinona como inhibidores de isocitrato deshidrogenasa mutante (mt-idh). |
ES2953347T3 (es) | 2014-09-19 | 2023-11-10 | Forma Therapeutics Inc | Derivados de piridin-2(1H)-ona quinolinona como inhibidores de isocitrato deshidrogenasa mutante |
ES2905564T3 (es) | 2014-12-22 | 2022-04-11 | Us Health | Inhibidores mutantes de IDH1 útiles para tratar el cáncer |
GB2533925A (en) | 2014-12-31 | 2016-07-13 | Univ Bath | Antimicrobial compounds, compositions and methods |
WO2016171756A1 (fr) | 2015-04-21 | 2016-10-27 | Forma Therapeutics, Inc. | Composés hétérocycliques de quinoléinone à cinq chaînons comme inhibiteurs de l'isocitrate déshydrogénase mutante |
WO2016171755A1 (fr) | 2015-04-21 | 2016-10-27 | Forma Therapeutics, Inc. | Dérivés de phénylquinoléinone en tant qu'inhibiteurs de l'isocitrate déshydrogénase mutante |
WO2017019429A1 (fr) | 2015-07-27 | 2017-02-02 | Eli Lilly And Company | Coposés de 7-phényléthylamino -4 h-pyrimido [4,5-d] [1,3] oxazin-2-one et leur utilisation en tant qu'inhibiteurs de idh1 mutante |
MX2018010261A (es) | 2016-02-26 | 2019-02-11 | Agios Pharmaceuticals Inc | Inhibidores de idh1 para el tratamiento de neoplasias malignas hematologicas y tumores solidos. |
US10696665B2 (en) | 2016-06-06 | 2020-06-30 | Eli Lilly And Company | Mutant IDH1 inhibitors |
CN109641887B (zh) | 2016-06-22 | 2022-09-20 | 美国政府健康及人类服务部 | 可用作用于治疗癌症的突变idh1抑制剂的噻唑衍生物 |
NZ754115A (en) | 2016-12-16 | 2021-07-30 | Lilly Co Eli | 7-phenylethylamino-4h-pyrimido[4,5-d][1,3]oxazin-2-one compounds as mutant idh1 and idh2 inhibitors |
-
2015
- 2015-09-18 ES ES20157755T patent/ES2953347T3/es active Active
- 2015-09-18 ME MEP-2020-78A patent/ME03776B/fr unknown
- 2015-09-18 NZ NZ73037315A patent/NZ730373A/en unknown
- 2015-09-18 IL IL292608A patent/IL292608A/en unknown
- 2015-09-18 BR BR112017005238-5A patent/BR112017005238B1/pt active IP Right Grant
- 2015-09-18 AU AU2015317329A patent/AU2015317329B2/en active Active
- 2015-09-18 EP EP23176702.1A patent/EP4257131A3/fr active Pending
- 2015-09-18 SI SI201530537T patent/SI3194376T1/sl unknown
- 2015-09-18 HU HUE20157755A patent/HUE062424T2/hu unknown
- 2015-09-18 MA MA040481A patent/MA40481A/fr unknown
- 2015-09-18 CN CN202311265288.0A patent/CN117695280A/zh active Pending
- 2015-09-18 MA MA053352A patent/MA53352A/fr unknown
- 2015-09-18 US US14/858,167 patent/US9834539B2/en active Active
- 2015-09-18 MY MYPI2017700895A patent/MY176250A/en unknown
- 2015-09-18 RS RS20200418A patent/RS60140B1/sr unknown
- 2015-09-18 FI FIEP20157755.8T patent/FI3733662T3/fi active
- 2015-09-18 EP EP20157755.8A patent/EP3733662B1/fr active Active
- 2015-09-18 PL PL15778433T patent/PL3194376T3/pl unknown
- 2015-09-18 PT PT15778433T patent/PT3194376T/pt unknown
- 2015-09-18 DK DK18198969.0T patent/DK3447050T3/da active
- 2015-09-18 WO PCT/US2015/051055 patent/WO2016044789A1/fr active Application Filing
- 2015-09-18 SG SG11201702194SA patent/SG11201702194SA/en unknown
- 2015-09-18 PL PL20157755.8T patent/PL3733662T3/pl unknown
- 2015-09-18 DK DK15778433.1T patent/DK3194376T3/en active
- 2015-09-18 LT LTEP15778433.1T patent/LT3194376T/lt unknown
- 2015-09-18 PT PT181989690T patent/PT3447050T/pt unknown
- 2015-09-18 KR KR1020177010585A patent/KR102209667B1/ko active IP Right Grant
- 2015-09-18 RS RS20181586A patent/RS58184B1/sr unknown
- 2015-09-18 ES ES18198969T patent/ES2790640T3/es active Active
- 2015-09-18 PL PL18198969T patent/PL3447050T3/pl unknown
- 2015-09-18 PT PT201577558T patent/PT3733662T/pt unknown
- 2015-09-18 PE PE2017000471A patent/PE20171056A1/es unknown
- 2015-09-18 HU HUE15778433A patent/HUE041460T2/hu unknown
- 2015-09-18 TW TW104131044A patent/TWI686390B/zh active
- 2015-09-18 EP EP15778433.1A patent/EP3194376B1/fr active Active
- 2015-09-18 LT LTEP18198969.0T patent/LT3447050T/lt unknown
- 2015-09-18 CN CN201580050441.5A patent/CN107001328B/zh active Active
- 2015-09-18 MX MX2017003404A patent/MX2017003404A/es active IP Right Grant
- 2015-09-18 CA CA2961817A patent/CA2961817C/fr active Active
- 2015-09-18 NZ NZ758641A patent/NZ758641A/en unknown
- 2015-09-18 CN CN202010391529.6A patent/CN111909130B/zh active Active
- 2015-09-18 JP JP2017515059A patent/JP6648115B2/ja active Active
- 2015-09-18 SI SI201531117T patent/SI3447050T1/sl unknown
- 2015-09-18 EA EA201790657A patent/EA034336B1/ru unknown
- 2015-09-18 MY MYPI2020001463A patent/MY197533A/en unknown
- 2015-09-18 ES ES15778433T patent/ES2704897T3/es active Active
- 2015-09-18 EP EP18198969.0A patent/EP3447050B1/fr active Active
-
2017
- 2017-03-07 US US15/452,256 patent/US20170174658A1/en not_active Abandoned
- 2017-03-14 IL IL251163A patent/IL251163B/en active IP Right Grant
- 2017-03-15 MX MX2019013203A patent/MX2019013203A/es unknown
- 2017-03-17 CL CL2017000658A patent/CL2017000658A1/es unknown
- 2017-03-17 PH PH12017500517A patent/PH12017500517A1/en unknown
- 2017-03-19 SA SA517381129A patent/SA517381129B1/ar unknown
- 2017-03-27 ZA ZA2017/02127A patent/ZA201702127B/en unknown
- 2017-04-03 CO CONC2017/0003241A patent/CO2017003241A2/es unknown
- 2017-04-13 EC ECIEPI201722933A patent/ECSP17022933A/es unknown
-
2018
- 2018-04-27 US US15/964,844 patent/US10414752B2/en active Active
-
2019
- 2019-01-21 CY CY20191100075T patent/CY1121149T1/el unknown
- 2019-03-01 US US16/290,240 patent/US10550098B2/en active Active
- 2019-04-17 ZA ZA2019/02446A patent/ZA201902446B/en unknown
- 2019-12-12 US US16/712,951 patent/US10889567B2/en active Active
- 2019-12-16 AU AU2019283765A patent/AU2019283765B2/en active Active
-
2020
- 2020-04-24 HR HRP20200666TT patent/HRP20200666T1/hr unknown
- 2020-05-04 CY CY20201100407T patent/CY1122865T1/el unknown
- 2020-11-23 US US17/101,018 patent/US11498913B2/en active Active
-
2021
- 2021-04-18 IL IL282363A patent/IL282363B/en unknown
- 2021-08-10 AU AU2021215141A patent/AU2021215141B2/en active Active
-
2022
- 2022-11-09 US US17/984,069 patent/US20230125739A1/en not_active Abandoned
-
2023
- 2023-11-09 US US18/506,060 patent/US20240150319A1/en active Pending
Also Published As
Similar Documents
Publication | Publication Date | Title |
---|---|---|
MA53352A (fr) | Dérivés de pyridin-2-(1h)-one-quinolinone en tant qu'inhibiteurs d'isocitrate déshydrogénase | |
MA47123A (fr) | Dérivés de benzooxazole en tant qu'mmunomodulateurs | |
MA47125A (fr) | Dérivés de pyrazole en tant qu'inhibiteurs de malt1 | |
MA40774A (fr) | Dérivés de diaryle-urée en tant qu'inhibiteurs de kinase p38 | |
MA45189A (fr) | Nouveaux dérivés hétérocycliques utiles en tant qu'inhibiteurs de shp2 | |
MA45244A (fr) | Pyridines substituées utilisées en tant qu'inhibiteurs de dnmt1 | |
MA55194A (fr) | Composés hétérocycliques en tant qu'immunomodulateurs | |
MA51878A (fr) | Composés d'aminothiazole en tant qu'inhibiteurs de c-kit | |
CL2016002736A1 (es) | Inhibidores de demetilasa-1 específico de lisina | |
MA40587A (fr) | Composés d'aminopyrimidinyle en tant qu'inhibiteurs de jak | |
MA46981A (fr) | Dérivés de benzimidazole en tant qu'inhibiteurs de bromodomaine | |
MA40943A (fr) | Pyrrolopyridines substituées utilisées en tant qu'inhibiteurs de bromodomaines | |
MA40940A (fr) | Pyrrolopyridines substituées utilisées en tant qu'inhibiteurs de bromodomaines | |
MA41140A (fr) | Dérivés de 2,4-dioxo-quinazoline-6-sulfonamide en tant qu'inhibiteurs de la parg | |
MA54253A (fr) | Procédé de préparation de dérivés de 2-chloro-4-hétéroaryl-pyridimidines | |
MA54567A (fr) | Pyridine et composés de pyridimine en tant qu'inhibiteurs de pi3k-gamma | |
DK3286177T3 (da) | Quinolinderivater som tam rtk-inhibitorer | |
MA46878A (fr) | Composés de benzodiazolium en tant qu'inhibiteurs d'enac | |
DK3261726T3 (da) | Sammensætning til behandling af acne | |
IL250038A0 (en) | 4,5 - dehydroisoxazole derivatives used as nampt inhibitors | |
DK3202766T3 (da) | Isoxazolderivat som muteret isocitratdehydrogenase 1-inhibitor | |
HK1253572A1 (zh) | 作為tnap抑制劑的吡啶並噁嗪酮化合物 | |
DK3216451T3 (da) | Oftalmisk vandig sammensætning | |
FR3023290B1 (fr) | Derives de flavaglines | |
MA41174A (fr) | Dérivés d'imidazopyridazine utilisés en tant qu'inhibiteurs de pi3kbeta |